Literature DB >> 24657775

Anatomical and functional pathways of rhythmogenic inspiratory premotor information flow originating in the pre-Bötzinger complex in the rat medulla.

N Koshiya1, Y Oku2, S Yokota3, Y Oyamada4, Y Yasui3, Y Okada5.   

Abstract

The pre-Bötzinger complex (preBötC) of the ventrolateral medulla is the kernel for inspiratory rhythm generation. However, it is not fully understood how inspiratory neural activity is generated in the preBötC and propagates to other medullary regions. We analyzed the detailed anatomical connectivity to and from the preBötC and functional aspects of the inspiratory information propagation from the preBötC on the transverse plane of the medulla oblongata. Tract-tracing with immunohistochemistry in young adult rats demonstrated that neurokinin-1 receptor- and somatostatin-immunoreactive neurons in the preBötC, which could be involved in respiratory rhythmogenesis, are embedded in the plexus of axons originating in the contralateral preBötC. By voltage-imaging in rhythmically active slices of neonatal rats, we analyzed origination and propagation of inspiratory neural activity as depolarizing wave dynamics on the entire transverse plane as well as within the preBötC. Novel combination of pharmacological blockade of glutamatergic transmission and mathematical subtraction of the video images under blockade from the control images enabled to extract glutamatergic signal propagations. By ultra-high-speed voltage-imaging we first demonstrated the inter-preBötC conduction process of inspiratory action potentials. Intra-preBötC imaging with high spatiotemporal resolution during a single spontaneous inspiratory cycle unveiled deterministic nonlinearities, i.e., chaos, in the population recruitment. Collectively, we comprehensively elucidated the anatomical pathways to and from the preBötC and dynamics of inspiratory neural information propagation: (1) From the preBötC in one side to the contralateral preBötC, which would synchronize the bilateral rhythmogenic kernels, (2) from the preBötC directly to the bilateral hypoglossal premotor and motor areas as well as to the nuclei tractus solitarius, and (3) from the hypoglossal premotor areas toward the hypoglossal motor nuclei. The coincidence of identified anatomical and functional connectivity between the preBötC and other regions in adult and neonatal rats, respectively, indicates that this fundamental connectivity is already well developed at the time of birth.
Copyright © 2014 IBRO. All rights reserved.

Entities:  

Keywords:  medulla oblongata; pre-Bötzinger complex; respiratory rhythm; rhythmically active slice; tract tracing; voltage-sensitive dye

Mesh:

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Year:  2014        PMID: 24657775     DOI: 10.1016/j.neuroscience.2014.03.002

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  13 in total

1.  Optogenetic excitation of preBötzinger complex neurons potently drives inspiratory activity in vivo.

Authors:  Zaki Alsahafi; Clayton T Dickson; Silvia Pagliardini
Journal:  J Physiol       Date:  2015-07-14       Impact factor: 5.182

2.  Midline section of the medulla abolishes inspiratory activity and desynchronizes pre-inspiratory neuron rhythm on both sides of the medulla in newborn rats.

Authors:  Hiroshi Onimaru; Kayo Tsuzawa; Yoshimi Nakazono; Wiktor A Janczewski
Journal:  J Neurophysiol       Date:  2015-02-25       Impact factor: 2.714

3.  Organotypic slice cultures containing the preBötzinger complex generate respiratory-like rhythms.

Authors:  Wiktor S Phillips; Mikkel Herly; Christopher A Del Negro; Jens C Rekling
Journal:  J Neurophysiol       Date:  2015-12-09       Impact factor: 2.714

Review 4.  Review: The past, present and future challenges in epilepsy-related and sudden deaths and biobanking.

Authors:  M Thom; M Boldrini; E Bundock; M N Sheppard; O Devinsky
Journal:  Neuropathol Appl Neurobiol       Date:  2018-02       Impact factor: 8.090

Review 5.  Temporal variations in the pattern of breathing: techniques, sources, and applications to translational sciences.

Authors:  Yoshitaka Oku
Journal:  J Physiol Sci       Date:  2022-08-29       Impact factor: 2.257

6.  MRI and pathology correlations in the medulla in sudden unexpected death in epilepsy (SUDEP): a postmortem study.

Authors:  S Patodia; M Tachrount; A Somani; I Scheffer; T Yousry; X Golay; S M Sisodiya; M Thom
Journal:  Neuropathol Appl Neurobiol       Date:  2020-07-15       Impact factor: 8.090

7.  Diving Response in Rats: Role of the Subthalamic Vasodilator Area.

Authors:  Eugene V Golanov; James M Shiflett; Gavin W Britz
Journal:  Front Neurol       Date:  2016-09-21       Impact factor: 4.003

8.  Capsaicin Enhances Glutamatergic Synaptic Transmission to Neonatal Rat Hypoglossal Motor Neurons via a TRPV1-Independent Mechanism.

Authors:  Prajwal P Thakre; Mark C Bellingham
Journal:  Front Cell Neurosci       Date:  2017-12-05       Impact factor: 5.505

Review 9.  The respiratory control mechanisms in the brainstem and spinal cord: integrative views of the neuroanatomy and neurophysiology.

Authors:  Keiko Ikeda; Kiyoshi Kawakami; Hiroshi Onimaru; Yasumasa Okada; Shigefumi Yokota; Naohiro Koshiya; Yoshitaka Oku; Makito Iizuka; Hidehiko Koizumi
Journal:  J Physiol Sci       Date:  2016-08-17       Impact factor: 2.781

10.  Change in network connectivity during fictive-gasping generation in hypoxia: prevention by a metabolic intermediate.

Authors:  Andrés Nieto-Posadas; Ernesto Flores-Martínez; Jonathan-Julio Lorea-Hernández; Ana-Julia Rivera-Angulo; Jesús-Esteban Pérez-Ortega; José Bargas; Fernando Peña-Ortega
Journal:  Front Physiol       Date:  2014-07-23       Impact factor: 4.566

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